Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Vertebral Technologies with 7 510(k) clearances and 1 device recall. The most recent is a device recall dated Jan 13, 2017: InterFuse Tail Traction Tool, Part Number 9116. The InterFuse Tail Traction Tool is an ….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Jan 13, 2017 | InterFuse Tail Traction Tool, Part Number 9116. The InterFuse Tail Traction Tool is an optional Class I non-sterile reusable instrument thaClass II · Fit issues have been identified with the Tail Traction Tool (PN 9116) when used with the Interfuse T tailed implant. Th | Device recalls |
| Sep 3, 2013 | INTERFUSE L INTERVERTEBRAL BODY FUSION DEVICEK131540 · MAX | 510(k) clearances |
| May 27, 2011 | INTERFUSE T INVERTEBRAL BODY FUSION DEVICEK110226 · MAX | 510(k) clearances |
| Feb 3, 2011 | INTERFUSE DA INVERTEBRAL BODY FUSION DEVICEK110045 · MAX | 510(k) clearances |
| Oct 6, 2010 | INTERFUSE T INVERTEBRAL BODY FUSION DEVICEK102277 · MAX | 510(k) clearances |
| Dec 23, 2009 | INTERFUSE INVERTEBRAL BODY FUSION DEVICE MODEL 9076K093675 · MAX | 510(k) clearances |
| Jul 30, 2009 | MODIFICATION TO: INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE , MODEL 9076K091988 · MAX | 510(k) clearances |
| Jun 10, 2008 | INTERFUSE INTERVERTEBRAL BODY FUSION DEVICEK080673 · MAX | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
